Luca Stefanucci

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 4

Top Topics

Genome Wide Association Study

Pulmonary Embolism

Circulating Tumor

Top Venues

Journal of thrombosis and haemostasis : JTH

Nature communications

This page only lists publications with an associated author ORCID identifier.

Publications

Luca Stefanucci, Janine H Collins, Matthew Christopher Sims, Iñigo Barrio-Hernandez, Luanluan Sun, Oliver S Burren, Livia Perfetto, Isobel Bender, Tiffany J Callahan, Kathryn Fleming, Jose Antonio Guerrero, Henning Hermjakob, Maria Jesus Martin, James David Stephenson, Kalpana Panneerselvam, Slavé Petrovski, Pablo Porras, Peter Nick Robinson, Quanli Wang, Xavier Watkins, Mattia Frontini, Roman A Laskowski, Pedro Beltrao, Emanuele Di Angelantonio, Keith Gomez, Michael A Laffan, Willem Hendrik Ouwehand, Andrew D Mumford, Kathleen Freson, Keren Jacqueline Carss, Kate Downes, Nicholas S Gleadall, Karyn Megy, Elspeth A Bruford, Dragana Vuckovic
The effects of pathogenic variants for inherited hemostasis disorders in 140,214 UK Biobank participants. Blood (2023)
Parsa Akbari, Dragana Vuckovic, Luca Stefanucci, Tao Jiang, Kousik Kundu, Roman Kreuzhuber, Erik L Bao, Janine H Collins, Kate Downes, Luigi Grassi, Jose Antonio Guerrero, Stephen Kaptoge, Julian C Knight, Stuart Meacham, Jennifer Sambrook, Denis Seyres, Oliver Stegle, Jeffrey M Verboon, Klaudia Walter, Nicholas A Watkins, John Danesh, David J Roberts, Emanuele Di Angelantonio, Vijay G Sankaran, Mattia Frontini, Stephen Burgess, Taco Kuijpers, James E Peters, Adam S Butterworth, Willem Hendrik Ouwehand, Nicole Soranzo, William John Astle
A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Nature communications 14 (1) (2023)
Luca Stefanucci, Mattia Frontini
Non-coding genetic variation in regulatory elements determines thrombosis and hemostasis phenotypes. Journal of thrombosis and haemostasis : JTH 20 (8) (2022)
Pierre-Emmanuel Morange, Franck Peiretti, Lénaïck Gourhant, Carole Proust, Omar Soukarieh, Anne-Sophie Pulcrano-Nicolas, Ganapathi Varma Saripella, Luca Stefanucci, Romaric Lacroix, Manal Ibrahim-Kosta, Catherine A Lemarié, Mattia Frontini, Marie-Christine Alessi, David Alexandre Trégouët, Francis Couturaud
A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant. PLoS genetics 17 (1) (2021)